Systems and methods for treatment of prostatic tissue

ABSTRACT

A prostate therapy system is provided that may include any of a number of features. One feature of the prostate therapy system is that it can access a prostate lobe transurethrally. Another feature of the prostate therapy system is that it can deliver condensable vapor into the prostate to ablate the prostate tissue. Another feature of the prostate therapy system is that it can aspirate tissue from the prostate. Yet another feature of the prostate therapy system is that it includes a cutter that can rotate during delivery of vapor and aspiration of tissue. Methods associated with use of the prostate therapy system are also covered.

CROSS REFERENCE TO RELATED APPLICATIONS

This application claims the benefit under 35 U.S.C. 119 of U.S.Provisional Patent Application No. 61/144,648, filed Jan. 14, 2009,titled “Systems and Methods for Treatment of Prostatic Tissue,” U.S.Provisional Patent Application No. 61/144,654, filed Jan. 14, 2009,titled “Medical Systems and Methods,” and U.S. Provisional PatentApplication No. 61/146,234, filed Jan. 21, 2009, titled “Medical Systemsand Methods.” These applications are herein incorporated by reference intheir entirety.

INCORPORATION BY REFERENCE

All publications and patent applications mentioned in this specificationare herein incorporated by reference to the same extent as if eachindividual publication or patent application was specifically andindividually indicated to be incorporated by reference.

FIELD OF THE INVENTION

The present invention relates to an apparatus and a related method forthe minimally invasive treatment of prostate tissue.

BACKGROUND OF THE INVENTION

Several systems and methods have been developed or proposed for thetreatment of prostate tissue to alleviate BPH symptoms or to treatprostate tissue. For example, tissue ablation methods have been based onRF ablation, microwave ablation, high intensity focused ultrasound(HIFU), cryoablation, radiation, surgery, and brachytherapy. Surgicalmethods with and without robotic assistance have been developed forremoval of diseased prostate tissue.

The apparatus, techniques and methods disclosed herein are adapted tofor the treatment of prostate tissue in general and more particularlyare focused on treatment of BPH (benign prostatic hyperplasia) andprostate cancer. BPH is a common problem experienced by men over about50 years old that relates to urinary tract obstruction. Prostatichyperplasia or enlargement of the prostate gland leads to compressionand obstruction of the urethra which results in symptoms such as theneed for frequent urination, a decrease in urinary flow, nocturia anddiscomfort.

Ablation of prostatic tissue with electromagnetic energy is well knownand has the advantage of allowing a less invasive approach. For example,high-frequency current in a electrosurgical ablation or prostatic tissuecauses cell disruption and cell death. Tissue resorption by the body'swound healing response then can result in a volumetric reduction oftissue that may be causing urinary tract obstruction. One disadvantageor high-frequency current of laser ablation is potential tissuecarbonization that results in an increased inflammatory response and farlonger time to heal following the ablation.

SUMMARY OF THE INVENTION

A method for treating a prostate disorder comprises inserting a probeinto prostatic tissue, rotating a cutter to volumetrically removeprostatic tissue in at least one lobe of the prostate, substantiallywithout damage to the urethra, and delivering a vapor from the probe toseal a margin of the removed prostatic tissue.

In some embodiments, the delivering step applies sufficient thermalenergy to substantially modify tissue. The modification of tissue cancomprise weakening covalent bonds, denaturing proteins, or disruptingcollagen structures, for example.

In some embodiments, the method comprises imaging the ablation probe.

In one embodiment, an applied energy from the vapor is betweenapproximately 100 W and 1000 W. In another embodiment, betweenapproximately 10 grams and 50 grams of prostatic tissue are removedduring the rotating step.

In some embodiments, an energy release from a phase change in the vaporseals the margin of the removed prostatic tissue.

Another method for treating a prostate disorder is provided, comprisingintroducing a tissue cutting instrument into prostatic tissue, actuatingthe tissue cutting instrument and a negative pressure source to cut andextract prostatic tissue, and delivering a condensable vapor into theprostatic tissue.

In some embodiments, the delivering step applies sufficient thermalenergy to substantially modify tissue. The modification of tissue cancomprise weakening covalent bonds, denaturing proteins, or disruptingcollagen structures, for example.

In one embodiment, the delivering step applies sufficient thermal energyto seal or coagulate margins of the extracted prostatic tissue.

In some embodiments, the method further comprises imaging the ablationprobe.

In one embodiment, an applied energy from the vapor is betweenapproximately 100 W and 1000 W. In another embodiment, betweenapproximately 10 grams and 50 grams of prostatic tissue are removedduring the rotating step.

In one embodiment, an energy release from a phase change in the vaporseals the margin of the removed prostatic tissue during the deliveringstep.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a vapor energy delivery system and more particularly acut-away view of a handle portion of an instrument with an inductiveheating assembly for applying vaporization energy to a fluid flowtogether with a looped flow system for maintaining a circulating flow ofhigh energy vapor which is releasable on demand to flow through anextension member to interact with tissue.

FIG. 2 is a schematic view of the inductive heating assembly of FIG. 1.

FIG. 3 is a schematic view of a patient prostate and a first step ofintroducing a tissue-selective extraction device into a patient urethra,showing tissue volumes targeted for ‘coring’ or extraction.

FIG. 4 is a schematic view of the patient prostate of FIG. 3 with asubsequent step of introducing the working end or the tissue-selectiveextraction device into a proximal aspect of the prostate and through theprostate adjacent the urethra.

FIG. 5 is a sectional view of the working end of FIG. 4 illustratingschematically how tissue is selectively extracted.

FIG. 6 is a schematic view of another instrument working end.

FIG. 7 is a schematic view of another instrument working end.

FIG. 8 is a schematic view of another instrument working end.

FIG. 9 is a schematic view of another instrument working end.

FIG. 10 is a schematic view of another instrument working end.

FIG. 11 is a schematic view of a high speed rotational cutter with vaporsealing functionality illustrating a method of the invention in removingand sealing prostate tissue.

FIG. 12 is a schematic view of the working end of the high speedrotational cutter of FIG. 11 with vapor sealing functionality forremoving prostate tissue.

DETAILED DESCRIPTION OF THE INVENTION

The present invention provides for a vapor energy generation system thatcan be configured for introduction into a patient's urethra or prostate,or can be configured to access prostatic tissue trans-rectally orendoscopically. The system is configured to deliver a heated vapor, forexample water vapor, to tissue as described in the following U.S. PatentApplications: U.S. application Ser. No. 10/681,625, filed Oct. 7, 2003,now U.S. Pat. No. 7,674,259, titled “Medical Instruments and Techniquesfor Thermally-Mediated Therapies”; U.S. application Ser. No. 11/158,930,filed Jun. 22, 2005, now U.S. Pat. No. 7,892,229, titled “MedicalInstruments and Techniques for Treating Pulmonary Disorders”; U.S.application Ser. No. 11/244,329, filed Oct. 5, 2005, now U.S. Pat. No.8,016,823, titled “Medical Instrument and Method of Use”; and U.S.application Ser. No. 11/329,381, filed Jan. 10, 2006, titled “MedicalInstrument and Method of Use”.

The generation and delivery of a collapsible, high energy vapor forvarious therapeutic procedures is further disclosed in systems with“remote” vapor generation systems or sources in co-pending ProvisionalPatent Application Nos. 60/929,632, 61/066,396, 61/068,049, or withvapor generator in a handle or working end, or combination thereof, asdescribed in Provisional Patent Application Nos. 61/068,130, 61/123,384,61/123,412, 61/126,651, 61/126,612, 61/126,636, 61/126,620.

FIG. 1 illustrates a vapor energy generation system 800 having a handle802 comprising an inductive heating system similar to that described inProvisional Application Nos. 61/123,416; 61/123,417; and 61/126,647. InFIG. 1, the handle 802 is coupled by temperature resistant fitting 806to a pressurized liquid or fluid source 810 that delivers liquid at acontrolled flow rate and pressure. The liquid flow passes through avapor generating inductive heater 805 coupled to an electrical sourceand controller 820. The system and handle is configured for a loopedliquid/vapor flow to provide vapor to working end or exit channel 822 todeliver the vapor to a tissue site. The system has inflow channelindicated at 824 and outflow channel at 826 that can communicate with acollection reservoir 830 and/or a negative pressure source 835. A valve836, for example, operated by a footswitch is provided in outflowchannel 826 to re-direct vapor into the exit channel 822 and extensionmember 840.

A vapor energy generation system 800 as shown in FIG. 1 can be used forany surgical/medical application, with the extension member 840comprising an elongate ablation probe, a needle, a flexible catheter, orother similar elongate delivery devices. This system can be used for acatheter for delivering energy for endovascular applications, fortreating respiratory tract disorders, for endometrial ablationtreatments or for needle ablation treatments. In the embodiment of FIG.1, an optional secondary heater 845 is shown with a concentric insulator846. This secondary heater can add further vaporization energy to vaporthat starts to flow through exit channel 822. The secondary heater canbe an inductive heater or a resistive heater that uses a microporousmaterial to provide a large surface area to apply energy to the vapor toremove any water droplets. This system can provide a vapor that is atleast 90% water vapor. The secondary heater is operatively coupled tothe electrical source and controller 820 by electrical leads (notshown).

FIG. 2 illustrates a vapor generating inductive heater 805 that in oneembodiment comprises a ceramic cylinder 850 with a bore 852 therein. Theceramic cylinder 850 can be approximately 1.0″ to 1.5″ in length and0.25″ in diameter with a 0.10″ bore 852, for example. The bore 852 canbe packed with a plurality of small diameter hypotubes 855 that aremagnetic responsive, such as 316 stainless steel, for example. In oneembodiment, the hypotubes 855 are 0.016 thin wall tubes. A winding 860of one to ten layers having and an axial length of about 1.0″ can beprovided about the ceramic cylinder 850 for inductive heating of thehypotubes 855 using very high frequency current from an electricalsource. In one embodiment the winding 860 can be 26 Ga. Copper wire witha Teflon coating. It has been found that delivering at least 50 W, 100W, 200 W, 300 W, 400 W, or 600 W with suitable flow rates of water canproduce very high quality vapor, for example 90% vapor and better.

In FIG. 2, it can be seen that an inductively heated hypotube 855′ alsocan be spiral cut to provide flexibility for such an inductive heater tobe positioned in a catheter or probe working end. For example, suchflexible heatable elements can be carried in the bore of a flexible hightemperature resistant polymeric insulative member such to provide aflexible catheter that is configured for endovascular navigation. Aninsulation layer about an exterior of the inductive heater is not shown.In general, the vapor generating inductive heater 805 can configured toprovide a high quality vapor media with precise parameters in terms ofvapor quality, exit vapor pressure from a working end, exit vaportemperature, and maintenance of the parameters within a tight range overa treatment interval. All these parameters can be controlled with a highlevel of precision to achieve controlled dosimetry, whether theparticular treatment calls for very low pressures (e.g., 1-5 psi) orvery high pressures (200 psi or greater) over a treatment interval, andwhether the treatment interval is in the 1-10 second range or 2 to 5minute range.

Now turning to FIGS. 3-4, a system including an elongated introducer 102with imaging system 104 is introduced into a patient urethra 105 withinprostate 106 and navigated to a predetermined location wherein thedistal end of the instrument and imaging system 104 can identifyanatomical landmarks. In one embodiment, the introducer 102 has an axialchannel 110 that carries an extendable ablation probe 115, as shown inFIG. 4. In FIG. 3, it can be seen that tissue region or cores 120A and120B in the opposing lobes of the prostate are targeted for removaltogether with thermal sealing of the margins of the extracted tissuevolumes. The ablation probe 115 is adapted to be insertedtransurethrally into a prostate lobe of a male subject to delivercondensable vapor to the prostate lobe and aspirate prostate tissueproximally into the ablation probe.

Referring to FIG. 4, the ablation probe 115 has a working end 125 thatis configured for applying mechanical and thermal energy to prostatetissue for ablation and volumetric removal of the tissue adjacent theurethra. The working end can be from about 2 to 6 mm in diameter, forexample. The working end 125 can be translated axially back and forthwithin the prostate to ablate and remove tissue in a method depicted inFIG. 5. In addition, referring back to FIG. 4, the ablation probe isoperatively coupled to vapor source 100, aspiration 180, and controller185. The vapor source 100 can be a condensable vapor source, such as thevapor energy generation system described above in FIG. 1. Aspiration 180can be a negative pressure or vacuum source to provide suction to theablation probe, and controller 185 can be used to control the deliveryof vapor to a patient as well as the aspiration of tissue from thepatient. The controller can comprise a computer or CPU and controls(e.g., a joystick, buttons or levers on the proximal end of the ablationprobe, a mouse/keyboard, etc) for use by a physician to control vapordelivery and suction during the surgical procedure.

The instrument working end 125 is shown in sectional view in FIG. 5where it can be seen that a vapor system or source 100 (such as a sourcedescribed in FIG. 1) is fluidly coupled to at least one vapor inflowchannel 160 that extends to at least one vapor delivery port 164 in arecess 165 of the distal end of the device. The axis of each vapordelivery port can be directed non-axially relative to the axis 170 theinstrument and the axes are directed inward toward the device axis 170.The axes of vapor ejection can have an angle 172 of between about 10° to90° relative to axis 170.

Still referring to FIG. 5, the ablation probe 115 has an aspiration port175 in fluid communication with an aspiration or negative pressuresource 180 and a controller (not illustrated) for suctioning tissue intothe working end recess 165 and extracting vapor and tissue detritus. Theaspiration port is adapted to aspirate prostate tissue proximally intothe ablation probe. In use, it can be understood that high pressureinjection of vapor from ports 164 as depicted in FIG. 5 will causethermal damage, weakening and denaturation of proteins and tissueconstituents while at the same time the vapor and water droplets thereincan apply sufficient mechanical forces to disintegrate andvolumetrically remove tissue at the vapor-tissue interface. In oneembodiment, the quality of the vapor, or combination of jetted vaporwith jetted water droplets can cut the thermally weakened tissue.

Referring to FIGS. 3-5, it can be understood how translating the workingend 125 axially while actuating the vapor flow and negative pressuresource can core out volumes in prostatic tissue (FIG. 3). Additionally,referring to FIG. 4, the working end 125 can be rotated during vapordelivery and aspiration for additional coring. Rotation of the workingend can be manual (e.g., physical rotation of the instrument by thephysician) or, alternatively, a rotating mechanism 186 (e.g., a poweredrotating motor) can be coupled to the working end 125 to automaticallyrotate the distal end of the device during ablation and aspiration. Therotating mechanism can be configured to rotate the ablation probebetween 5 rpm and 10,000 rpm, for example. Further details of a methodof rotating an ablation probe in tissue are describe in U.S. patentapplication Ser. Nos. 12/389,808 and 61/123,416, which are incorporatedherein by reference.

The vapor flow and phase change energy release contemporaneously sealsor coagulated the tissue margins to prevent bleeding. Following thetreatment, the body's wound healing response return the prostate to ahealed condition more rapidly than other methods that ablate a similartissue volume in situ, since the tissue burden to be resorbed is greatlyreduced. In order to advance the working end 125 through the wall of theurethra, a sharp-tipped sleeve (not shown) may be used to penetrate thewall of the lumen.

FIG. 6 illustrates another embodiment similar to that of FIG. 5 withworking end 125′ having similar functionality with the tissue receivingand ablation structure being oriented at an angle relative to the axisof the device. The angled working surface is thus adapted to ablate,disintegrate and extract tissue somewhat to the side of the device and amethod of use included low speed or high speed rotation in conjunctionwith axial translation.

FIG. 7 illustrates another embodiment similar to that of FIGS. 5-6 withworking end 125″ having similar functionality with the tissue receivingand ablation structure being oriented at a side of the extension membersubstantially parallel to the axis of the device. The side extractionport is thus adapted to ablate, disintegrate and extract tissue and amethod of use included low speed or high speed rotation in conjunctionwith axial translation.

FIG. 8 illustrates another embodiment similar to that of FIGS. 5-7 withworking end 200 that again is adapted to ablate, disintegrate andextract tissue at a side of the extension member substantially parallelto the axis of the device. In this embodiment, the system includes avery high pressure liquid fluid jetting source 220 that communicateswith a liquid ejection port 225 in the working end wherein the ejectedliquid is capable of disintegrated, obliterating or cutting tissue. Thesystem also includes a vapor source as described previously for ejectinghigh temperature vapor from at least one port to seal the margins of thedisintegrated tissue.

FIG. 9 illustrates another embodiment similar to working end 200 that isadapted to ablate, disintegrate and extract tissue at a side of theextension member similar to that of FIG. 8. The embodiment of FIG. 9 hasa high pressure liquid fluid jetting source 220 with a liquid ejectionport 225 that is directed outward from the axis of the device. The vapordelivery port is similarly oriented. In a method of use, the working endcan be rotated at high speed, as described above in FIG. 4, to insurethat the fluid jet only cuts or disintegrates tissue to a controlled,limited depth.

FIG. 10 illustrates another embodiment of working end 250 that isadapted to ablate, disintegrate and extract tissue similar to that ofFIG. 8. The embodiment of FIG. 10 has a high pressure liquid fluidjetting source 220 with liquid ejection port(s) that are leading theaspiration port when rotated at high speed. The vapor delivery port(s)are exposed to lag behind the aspiration port when rotating at any highspeed from about 5 rpm to 10,000 rpm. In one method, the fluid jet ispulsed at a rate of 1 to 100 pulses/second. In another embodiment, thefluid jetting is pulsed with intermittent pulses of water and vapor at ahigh repetition rate with the jetted water aliquot capable ofdisintegrating tissue and the vapor aliquot configured to weaken tissueand thermally seal tissue.

In another embodiment, the working end can carry first and secondoutlets for jetting with axes that at angled to intersect to cause acontrolled depth disintegration of tissue.

FIGS. 11 and 12 illustrate another embodiment of an ablation probe 402,including a working end 400 that includes at least one vapor port oroutlet 404, a high speed rotational cutter/shaver 406, and at least oneextraction port 414. FIG. 11 illustrates the probe inside a prostate ina region of prostatic tissue 405 targeted for ablation and removal.Referring to FIG. 12, the probe 402 comprises an elongate shaft 410. Inone embodiment, the source of vapor 100 is in fluid communication withvapor ports 404 disposed in the elongate shaft.

As shown in FIG. 12, the elongate shaft 410 can include cutouts 412along the working end of the shaft. The cutouts 412 can expose theinterior of the elongate shaft to reveal the high speed rotationalcutter/shaver 406 having an extraction port(s) 414, the cutter beingdisposed within the elongate shaft. In FIG. 12, an outer diameter of thehigh speed rotational cutter is sized and shaped to fit precisely withinan inner diameter of the elongate shaft. A high speed rotation mechanism460 can be coupled to the rotational cutter 406 and be configured torotate the rotational cutter within the elongate shaft. The high speedrotation mechanism 460 can be an air motor, electric motor or the likethat can rotate and or oscillate the cutting component/blade at fromabout 50 rpm to 20,000 rpm and in one embodiment can have theconfiguration of an orthopedic cutter/shaver known in the art. Againreferring to FIG. 12, the rotational cutter can include an extractionport in communication with an aspiration source 180. The aspirationsource can provide vacuum or negative pressure to the extraction port(s)for removal of tissue.

In use, the probe 402 can deliver heated vapor to tissue through vaporports 404. During delivery of vapor, rotation mechanism 460 can rotatecutter 406 within elongate shaft 410. The extraction port(s) 414 andaspiration source or negative pressure source 180 can apply a vacuum ornegative pressure to tissue, causing the tissue to be drawn into theextraction port and rotational cutter. As the rotational cutter 406rotates, the tissue can be cut from the body and extracted through theelongate shaft of the probe. In some embodiments, the cutouts 412 in theelongate shaft can be sharpened or serrated to increase the cuttingability of the probe. Thus, delivery of vapor to tissue through thevapor port(s) is configured to weaken tissue, and the extraction port(s)and rotational cutter are configured to cut tissue and aspirate tissueaway from the body. Continued delivery of vapor to tissue after cuttingcan then seal the tissue about the margins of the cut tissue.

In general, a method for treating a disorder of the prostate comprisesvolumetrically removing prostatic tissue in at least one lobesubstantially without damage to the patient urethra. The method ofvolumetrically removing tissue can be performed with the ejection of aheated fluid such as a condensable vapor from a device working end andaspiration of the disintegrated tissue. In one aspect of the invention,the ejection of fluid media applies sufficient thermal energy tosubstantially modify tissue, wherein the modification consists of atleast one of weakening covalent bonds, denaturing proteins anddisrupting collagen structures. Further, the ejection of fluid mediaapplies sufficient mechanical energy for tissue removal wherein removalconsists of at least one of disintegrating, cutting, excising andablating tissue. In another aspect of the invention, the ejection offluid media applies sufficient thermal energy to seal or coagulatemargins of the removed tissue. Also, the methods of volumetricallyremoving tissue can be performed contemporaneous with imaging, such asultrasound imaging.

In general, a method for treating a prostate disorder comprisesvolumetrically removing prostatic tissue radially outward from theurethra in at least one lobe while maintaining urethral patency. Themethod volumetrically removes tissue with the ejection of a heated vapormedia from a device working end and aspiration of the disintegratedtissue. The method applies energy to the prostate from the injectedcondensable vapor that is equal to at least 100 W, 250 W, 500 W, and1000 W. In another embodiment, injecting condensable vapor into theprostate delivers between 100 cal/gram and 600 cal/gram to the prostate.

In general, a method for treating a prostate disorder comprisesvolumetrically removing prostatic tissue equaling at least 10 grams, atleast 20 grams, at least 30 grams, at least 40 grams, and at least 50grams. In another embodiment, between 1 gram and 100 grams of prostatetissue can be removed. The method includes thermally coagulating themargins about the removed tissue. A method of the invention comprisescutting and extracting at least one region of prostatic tissue whilemaintaining urethral patency.

In one embodiment, a method of treating a disorder of the prostatecomprises introducing an ablation probe transurethrally in the prostate.In one embodiment, a high temperature condensable vapor can be deliveredto the prostate from a fluid or vapor source external to the ablationprobe through vapor ports disposed in an elongate shaft of the ablationprobe. A cutter disposed within the elongate shaft of the ablation probecan be rotated to cut tissue. In some embodiments, the cutter is rotatedto cut tissue before delivery of vapor. The cutter can include anextraction port. Vacuum or negative pressure can be applied to theextraction port to aspirate tissue proximally through the extractionport of the ablation probe. A core of prostate tissue can be removedwith this method. In some embodiments, the cutter is rotated whiletissue is extracted through the extraction ports. In some embodiments,the cutter can be rotated during delivery of vapor and aspiration oftissue. In another embodiment, the cutter is rotated and tissue isremoved, and then vapor is delivered to the margins of tissue to sealthe margins of removed tissue. In some embodiments, the margins ofremoved tissue are sealed with continued delivery of the hightemperature vapor. In other embodiments, a high pressure liquid insteadof a vapor can be injected through the ablation probe into the prostate.

To gain access to the prostate, an introducer can be introduced into theurethra, and the ablation probe can be advanced through the introducer.The ablation probe can then be advanced into an apex of a lobe of theprostate.

A system comprises an elongated tissue extraction member with a workingend configured for interstitial penetration in a patient prostate, avapor source in fluid communication with vapor delivery ports in thedistal end, a cutter disposed within the working end, and a negativepressure source coupled to a channel in fluid communication with atissue extraction port in the cutter. The vapor delivery port(s) can beoriented distally relative to an axis of the tissue extraction member,or at an angle relative to an axis of the tissue extraction member, ororiented at a side of tissue extraction member substantially parallel tothe axis of the tissue extraction member.

In one embodiment, a prostate therapy system comprises a condensablevapor source, an ablation probe adapted to be inserted transurethrallyinto a prostate lobe of an adult male human subject, the ablation probehaving a vapor delivery port communicating with the vapor source andadapted to deliver condensable vapor to the prostate lobe, and a cutterhaving an aspiration port adapted to cut and aspirate prostate tissueproximally into the ablation probe.

Another system comprises an elongate tissue extraction member with aworking end configured for interstitial penetration in a patientprostate, a vapor source in fluid communication with at least one vapordelivery ports in the distal end for applying thermal energy to tissue,and a high pressure liquid jetting source in communication with anoutlet in the distal end for disintegrating tissue. The system furtherincludes a negative pressure source coupled to a channel in fluidcommunication with a tissue extraction port in the working end.

In general, the methods of the invention include delivery of acondensable vapor that undergoes a phase change to provide appliedenergy of at least 250 cal/gm, 300 cal/gm, 350 cal/gm, 400 cal/gm and450 cal/gm of the vapor.

In another embodiment, the treatment with vapor can be accomplishedunder any suitable type of imaging. In one method, the steps can beviewed by means of ultrasound or x-ray imaging. In one method, theintroducer introduction and energy delivery methods of the invention canbe imaged by ultrasound system utilizing a trans-rectal ultrasoundsystem.

In another aspect of the invention, the system may contemporaneously beused to deliver fluids to targeted locations in the prostate for medicalpurposes, such as for general or localized drug delivery, chemotherapy,or injections of other agents that may be activated by vapor or heat.

As for additional details pertinent to the present invention, materialsand manufacturing techniques may be employed as within the level ofthose with skill in the relevant art. The same may hold true withrespect to method-based aspects of the invention in terms of additionalacts commonly or logically employed. Also, it is contemplated that anyoptional feature of the inventive variations described may be set forthand claimed independently, or in combination with any one or more of thefeatures described herein. Likewise, reference to a singular item,includes the possibility that there are plural of the same itemspresent. More specifically, as used herein and in the appended claims,the singular forms “a,” “and,” “said,” and “the” include pluralreferents unless the context clearly dictates otherwise. It is furthernoted that the claims may be drafted to exclude any optional element. Assuch, this statement is intended to serve as antecedent basis for use ofsuch exclusive terminology as “solely,” “only” and the like inconnection with the recitation of claim elements, or use of a “negative”limitation. Unless defined otherwise herein, all technical andscientific terms used herein have the same meaning as commonlyunderstood by one of ordinary skill in the art to which this inventionbelongs. The breadth of the present invention is not to be limited bythe subject specification, but rather only by the plain meaning of theclaim terms employed.

1. A method for treating a prostate disorder, comprising: inserting aprobe transurethrally into prostatic tissue; rotating a cutter tovolumetrically remove prostatic tissue in at least one lobe of theprostate, substantially without damage to the urethra; and delivering avapor from the probe to seal a margin of the removed prostatic tissue.2. The method of claim 1 wherein the delivering step applies sufficientthermal energy to substantially modify tissue.
 3. The method of claim 2wherein the modification of tissue comprises weakening covalent bonds.4. The method of claim 2 wherein the modification of tissue comprisesdenaturing proteins.
 5. The method of claim 2 wherein the modificationof tissue comprises disrupting collagen structures.
 6. The method ofclaim 1 further comprising imaging the ablation probe.
 7. The method ofclaim 1 wherein an applied energy from the vapor is betweenapproximately 100 W and 1000 W.
 8. The method of claim 1 wherein betweenapproximately 10 grams and 50 grams of prostatic tissue are removedduring the rotating step.
 9. The method of claim 1 wherein an energyrelease from a phase change in the vapor seals the margin of the removedprostatic tissue.
 10. A method for treating a prostate disorder,comprising: introducing a tissue cutting instrument transurethrally intoprostatic tissue; actuating the tissue cutting instrument and a negativepressure source to cut and extract prostatic tissue; and delivering acondensable vapor into the prostatic tissue.
 11. The method of claim 10wherein the delivering step applies sufficient thermal energy tosubstantially modify tissue.
 12. The method of claim 11 wherein themodification of tissue comprises weakening covalent bonds.
 13. Themethod of claim 11 wherein the modification of tissue comprisesdenaturing proteins.
 14. The method of claim 11 wherein the modificationof tissue comprises disrupting collagen structures.
 15. The method ofclaim 10 wherein the delivering step applies sufficient thermal energyto seal or coagulate margins of the extracted prostatic tissue.
 16. Themethod of claim 10 further comprising imaging the ablation probe. 17.The method of claim 10 wherein an applied energy from the vapor isbetween approximately 100 W and 1000 W.
 18. The method of claim 10wherein between approximately 10 grams and 50 grams of prostatic tissueare removed during the actuating step.
 19. The method of claim 10wherein an energy release from a phase change in the vapor seals themargin of the removed prostatic tissue during the delivering step.